Oncology Research Director: Lead Industry Trials

Plexus Partners Ltd; Gainesville (GA); On-site; USD 180,000 - 240,000; Full time

Benefits offered by this job

Relocation support

Full benefits

Malpractice insurance

CME allowance

Leadership exposure

Job summary

Plexus Partners Ltd. is seeking an Oncology Research Director / Principal Investigator to lead the Gainesville, GA oncology program on-site.

You will function as PI and Medical Director for industry-sponsored trials (Phase I–III), set feasibility and strategy with leadership, and ensure protocol conduct and safety with FDA/ICH-GCP compliance. The role demands an MD/DO with Georgia license, oncology board certification, and PI or sub-PI trial experience.

Qualifications

• MD/DO with active, unrestricted Georgia license or eligibility
• Board-certified in medical oncology or hematology/oncology
• Clinical trial experience as PI or sub-investigator on industry studies
• Established patient base or referral network is a plus
• Strong working knowledge of GCP, FDA regulations, and IRB processes

Responsibilities

• Lead the oncology research program at the Gainesville site as Principal Investigator and Medical Director
• Serve as PI on industry-sponsored oncology trials from Phase I to III
• Collaborate with leadership on feasibility, portfolio strategy and trial selection
• Oversee protocol conduct, subject safety and regulatory compliance
• Mentor sub investigators, advanced practice providers and coordinators as team grows
• Represent site with sponsors and CROs at meetings, site visits and audits

Skills

Oncology clinical trials experience

Leadership & mentorship

FDA/ICH-GCP knowledge

Education

MD/DO with Georgia license

Board certification in medical oncology or hematology/oncology

Job description

Plexus Partners Ltd. is seeking an Oncology Research Director / Principal Investigator to lead the Gainesville, GA oncology program on-site.

You will function as PI and Medical Director for industry-sponsored trials (Phase I–III), set feasibility and strategy with leadership, and ensure protocol conduct and safety with FDA/ICH-GCP compliance. The role demands an MD/DO with Georgia license, oncology board certification, and PI or sub-PI trial experience.